A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015564



Internal ID19104781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:127473502..127585807hg38UCSC Ensembl
Innerchr4:128394657..128506962hg19UCSC Ensembl
Innerchr4:128614107..128726412hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38112306
hg19112306
hg18112306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5384n100
Supporting Variantsnssv3639427
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015564
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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